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Biochemical Abnormality Associated with Smith-Lemli-Opitz Syndrome in an Infant with Features of Rutledge Multiple Congenital Anomaly Syndrome Confirms that the Latter Is a Variant of the Former

✍ Scribed by Dinesh Rakheja; Golder N. Wilson; Beverly B. Rogers


Publisher
Springer
Year
2003
Tongue
English
Weight
226 KB
Volume
6
Category
Article
ISSN
1093-5266

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